Superior integrin activating capacity and higher adhesion to fibrinogen matrix in buffy coat-derived platelet concentrates (PCs) compared to PRP-PCs

• Published in: Transfusion and apheresis science Vol. 57; no. 1; pp. 76 - 81
• Main Authors: Beshkar, Pezhman, Hosseini, Ehteramolsadat, Ghasemzadeh, Mehran
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.02.2018
• Subjects: Buffy coat (BC); Fibrinogen; Health technology assessment; Integrin alpha IIb beta 3 (αIIbβ3); Platelet adhesion; Platelet-rich plasma (PRP); Buffy coat (BC); Integrin alpha IIb beta 3 (αIIbβ3); Platelet adhesion; Platelet-rich plasma (PRP); Fibrinogen; Integrin alpha IIb beta 3 (α(IIb)β)
• ISSN: 1473-0502; 1878-1683
• DOI: 10.1016/j.transci.2017.12.003

Regardless of different sources, methods or devices which are applied for preparation of therapeutic platelets, these products are generally isolated from whole blood by the sedimentation techniques which are based on PRP or buffy coat (BC) separation. As a general fact, platelet preparation and storage are also associated with some deleterious changes that known as platelet storage lesion (PSL). Although these alternations in platelet functional activity are aggravated during storage, whether technical issues within preparation can affect integrin activation and platelet adhesion to fibrinogen were investigated in this study. PRP- and BC-platelet concentrates (PCs) were subjected to flowcytometry analysis to examine the expression of platelet activation marker, P-selectin as well as active confirmation of the GPIIb/IIIa (αIIbβ3) on day 0, 1, 3 and 5 post-storage. Platelet adhesion to fibrinogen matrix was evaluated by fluorescence microscopy. Glucose concentration and LDH activity were also measured by colorimetric methods. The increasing P-selectin expression during storage was in a reverse correlation with PAC-1 binding (r = −0.67; p = .001). PRP-PCs showed the higher level of P-selectin expression than BC-PCs, whereas the levels of PAC-1 binding and platelet adhesion to fibrinogen matrix were significantly lower in PRP-PCs. Higher levels of active confirmation of the GPIIb/IIIa in BC-PCs were also associated with greater concentration of glucose in these products. We demonstrated the superior capacities of integrin activation and adhesion to fibrinogen for BC-PCs compared to those of PRP-PCs. These findings may provide more advantages for BC method of platelet preparation.